Evidence map›Paper›PMID 41846895›Full record

ArticleFrontiers in medicine2026

miRNA-210 expression is associated with iron deficiency and biochemical parameters in hemodialysis patients.

Merve Kılıç, Hamad Dheir, Mahmud İslam, Zafer Ercan, Muhittin Abdulkadir Serdar

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Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Merve KılıçDepartment of Biochemistry and Molecular Biology, Graduate School of Health Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.
Hamad DheirDepartment of Nephrology, Sakarya University Faculty of Medicine, Sakarya, Türkiye.
Mahmud İslamDepartment of Nephrology, Sakarya University Faculty of Medicine, Sakarya, Türkiye.
Zafer ErcanDepartment of Nephrology, Sakarya University Training and Research Hospital, Sakarya, Türkiye.
Muhittin Abdulkadir SerdarDepartment of Biochemistry and Molecular Biology, Graduate School of Health Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: This study aimed to evaluate the potential of microRNA (miRNA)-210 as a biomarker for distinguishing iron deficiency anemia (IDA) from functional iron deficiency (FID) in hemodialysis (HD) patients. The diagnostic performance of miRNA-210 was also compared with conventional biochemical markers, including hemoglobin (Hb), ferritin, transferrin saturation (TSAT), and zinc protoporphyrin (ZnPP). Methods: Fifty HD patients were classified into control, IDA, and FID groups according to Hb, ferritin, and TSAT criteria. Pre-dialysis blood samples were collected, and plasma miRNA-210 levels were measured using reverse transcription quantitative polymerase chain reaction (RT Results: Plasma miRNA-210 levels were significantly higher in the IDA group compared to both the control ( Conclusion: miRNA-210 may serve as a supportive biomarker, reflecting the interaction between hypoxia and iron metabolism in distinguishing IDA from FID among HD patients. These findings indicate that miRNA-210 could provide additional value in understanding anemia pathophysiology and enhance diagnostic evaluation. Limitations: Key limitations include the small sample size, single-center, cross-sectional design, absence of a healthy control group, and lack of molecular-level functional validation. Larger multicenter studies are needed to confirm these findings and determine clinically relevant cut-off values for miRNA-210.

Indexed as

functional iron deficiencyhemodialysis patienthypoxiairon deficiency anemiamiRNA-210

Identifiers

PMID41846895
PMCPMC12989576

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